| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219111-137219220 | Common:1; Rare:34 | ||||
| chr6:137219245-137219525 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:137866941-137867285 | Rare:81 | ||||
| chr6:138404057-138405001 | Common:9; Rare:233 | ||||
| chr6:138773634-138773831 | Common:3; Rare:93 | ||||
| chr6:139028484-139028836 | Common:1; Rare:70 | ||||
| chr6:139374500-139374771 | Common:1; Rare:109 | ||||
| chr6:142147140-142147285 | Rare:52 | ||||
| chr6:143060688-143060935 | Common:7; Rare:90 | ||||
| chr6:143450651-143450991 | Common:1; Rare:119; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511647-143511772 | Common:4; Rare:31 | ||||
| chr6:143843196-143843473 | Common:2; Rare:95 | ||||
| chr6:144150413-144150592 | Common:2; Rare:49 | ||||
| chr6:144285242-144285642 | Common:2; Rare:96 | ||||
| chr6:144286141-144286546 | Common:6; Rare:76 |